1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

Base Information

Chemical Name:1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide
CAS No.:863441-31-0
Molecular Formula:C₂₅H₂₇FN₄O₅
Molecular Weight:482.512
Hs Code.:

Synonyms:1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

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Chemical Property of 1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

Chemical Property:

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Technology Process of 1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

There total 10 articles about 1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 863435-32-9
[7-[(4-fluorophenyl)methyl]-4-hydroxy-3-({[2-(methyloxy)ethyl]amino}carbonyl)-2-oxo-1,5-naphthyridin-1(2H)-yl]acetic acid

: 2516-34-9
cyclobutylamine

: 200731-31-3,148893-10-1
HATU

: 863441-31-0
1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide;

Reference yield:

: 863442-92-6
ethyl 3-amino-5-[(4-fluorophenyl)methyl]-2-pyridinecarboxylate

: 863441-31-0
1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: ethanol / Heating

1.2: 20 °C

2.1: O-(benzotriazol-1-yl)-N,N,N,N-tetramethyluroniumhexafluorophosphate; triethylamine / N,N-dimethyl-formamide

3.1: 1,2-dichloro-ethane / Heating

4.1: ethanol / Heating

With triethylamine; O-(benzotriazol-1-yl)-N,N,N,N-tetramethyluroniumhexafluorophosphate; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide; 3.2: |Dieckmann Condensation;
DOI:10.1016/j.bmcl.2014.05.011

Reference yield:

: 863443-07-6
N-{2-[(ethyloxy)carbonyl]-5-[(4-fluorophenyl)methyl]-3-pyridinyl}glycine

: 863441-31-0
1-[2-(Cyclobutylamino)-2-oxoethyl]-7-(4-fluorobenzyl)-4-hydroxy-N-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: O-(benzotriazol-1-yl)-N,N,N,N-tetramethyluroniumhexafluorophosphate; triethylamine / N,N-dimethyl-formamide

2: 1,2-dichloro-ethane / Heating

3: ethanol / Heating

With triethylamine; O-(benzotriazol-1-yl)-N,N,N,N-tetramethyluroniumhexafluorophosphate; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide; 2: |Dieckmann Condensation;
DOI:10.1016/j.bmcl.2014.05.011